Canonical Allele Identifier: CA2291756697

Gene: CHST9

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.27107360C= , CM000680.2:g.27107360C=	GRCh38
NC_000018.9:g.24687324C= , CM000680.1:g.24687324C=	GRCh37
NC_000018.8:g.22941322C=	NCBI36
NG_029856.1:g.82966G=

Transcript Alleles

HGVS	Amino-acid Change
NM_031422.6:c.121+35329G= MANE Select	NP_113610.2:n.121+35329G=
ENST00000618847.5:c.121+35329G= MANE Select	ENSP00000480991.1:n.121+35329G=
NM_001256316.1:c.121+35329G=	NP_001243245.1:n.121+35329G=
NM_001256316.2:c.121+35329G=	NP_001243245.1:n.121+35329G=
NM_001398493.1:c.121+35329G=	NP_001385422.1:n.121+35329G=
NM_031422.5:c.121+35329G=	NP_113610.2:n.121+35329G=
ENST00000580774.2:c.121+35329G=	ENSP00000464655.1:n.121+35329G=
ENST00000581714.5:c.121+35329G=	ENSP00000462852.1:n.121+35329G=
ENST00000618847.4:c.121+35329G=	ENSP00000480991.1:n.121+35329G=
XM_006722555.2:c.121+35329G=	XP_006722618.1:n.121+35329G=
XM_006722555.4:c.121+35329G=	XP_006722618.1:n.121+35329G=
XM_017026033.1:c.121+35329G=	XP_016881522.1:n.121+35329G=
XM_017026034.1:c.-148+35329G=	XP_016881523.1:n.-148+35329G=